Hulsey Daniel R, Hays Seth A, Khodaparast Navid, Ruiz Andrea, Das Priyanka, Rennaker Robert L, Kilgard Michael P
School of Behavioral Brain Sciences, The University of Texas at Dallas, 800 West Campbell Road, GR41, Richardson, TX 75080-3021, USA.
School of Behavioral Brain Sciences, The University of Texas at Dallas, 800 West Campbell Road, GR41, Richardson, TX 75080-3021, USA; Erik Jonsson School of Engineering and Computer Science, The University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080-3021, USA; Texas Biomedical Device Center, The University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080-3021, USA.
Brain Stimul. 2016 Mar-Apr;9(2):174-81. doi: 10.1016/j.brs.2015.12.007. Epub 2016 Jan 8.
Vagus nerve stimulation (VNS) paired with forelimb training drives robust, specific reorganization of movement representations in the motor cortex. The mechanisms that underlie VNS-dependent enhancement of map plasticity are largely unknown. The cholinergic nucleus basalis (NB) is a critical substrate in cortical plasticity, and several studies suggest that VNS activates cholinergic circuitry.
We examined whether the NB is required for VNS-dependent enhancement of map plasticity in the motor cortex.
Rats were trained to perform a lever pressing task and then received injections of the immunotoxin 192-IgG-saporin to selectively lesion cholinergic neurons of the NB. After lesion, rats underwent five days of motor training during which VNS was paired with successful trials. At the conclusion of behavioral training, intracortical microstimulation was used to document movement representations in motor cortex.
VNS paired with forelimb training resulted in a substantial increase in the representation of proximal forelimb in rats with an intact NB compared to untrained controls. NB lesions prevent this VNS-dependent increase in proximal forelimb area and result in representations similar to untrained controls. Motor performance was similar between groups, suggesting that differences in forelimb function cannot account for the difference in proximal forelimb representation.
Together, these findings indicate that the NB is required for VNS-dependent enhancement of plasticity in the motor cortex and may provide insight into the mechanisms that underlie the benefits of VNS therapy.
迷走神经刺激(VNS)与前肢训练相结合,可促使运动皮层中运动表征进行强大且特定的重组。VNS依赖性地图可塑性增强的潜在机制在很大程度上尚不清楚。胆碱能基底核(NB)是皮层可塑性的关键底物,多项研究表明VNS可激活胆碱能神经回路。
我们研究了NB对于VNS依赖性运动皮层地图可塑性增强是否是必需的。
训练大鼠执行压杆任务,然后注射免疫毒素192-IgG-皂草素以选择性损伤NB的胆碱能神经元。损伤后,大鼠进行为期五天的运动训练,在此期间VNS与成功的试验配对。行为训练结束时,使用皮层内微刺激来记录运动皮层中的运动表征。
与未训练的对照组相比,VNS与前肢训练相结合导致NB完整的大鼠近端前肢表征大幅增加。NB损伤阻止了这种VNS依赖性近端前肢区域的增加,并导致与未训练的对照组相似的表征。各组之间的运动表现相似,这表明前肢功能的差异不能解释近端前肢表征的差异。
总之,这些发现表明NB是VNS依赖性运动皮层可塑性增强所必需的,并且可能为VNS治疗益处的潜在机制提供见解。